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Cancer genomics

GNA5042

Synopsis

This unit will enable you to gain knowledge on the application of genome sequencing in the diagnoses and clinical management of cancer. You will learn about the different mechanisms that drive cancers and how integrative -omics can be applied to understanding cancer. You will learn about the types of somatic and germline cancer mutations that develop and how they are identified. You will apply genome curation techniques to analyse cancer genomes and learn how to identify clinically relevant sequence variants. The unit is designed to develop real-world skills in using cancer genome databases and generating clinical genome analysis reports.

Sourced from the Monash Handbook 2026.

Quick facts

Credit points
12
Level
5
Audience
Postgraduate
Type
Coursework
School
Faculty of Science
Faculty
School of Biological Sciences
Handbook year
2026

Prerequisites (1)

What it unlocks

Nothing in the visible graph depends on this unit.

Offerings (1)

  • First semesterClayton · ON-CAMPUS